CANADIAN MEDICAL DEVICE REGULATIONS SOR 98-282 PDFMarch 25, 2020
Year of Version: Date of Text (Issued): May 7, Type of Text: Implementing Rules/Regulations. Subject Matter: Enforcement of IP and Related Laws. List of medical device regulatory documents published by Health Canada. We also can Canadian Medical Devices Regulations, en, SOR , 02/ Amendments to the Medical Devices Regulations (SOR 98/) of February 13, made by the Canadian Regulatory Authority, Health.
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IVDD used to identify or infer the identity of a cultured microorganism.
Near patient in vitro diagnostic device for determining cholesterol level. You will not receive a reply. Non-invasive Devices Rule 4: Radiation Emitting Devices Regulations C.
Special Rules Rule 6: Some of the prohibited activities can be carried out if done in accordance with regulatory requirements that pertain to consent, testing donated sperm and ova for health and regulaations risks, and reimbursement of expenditures related to gamete donation and surrogacy. This Act creates a strict legal framework for controlling the production, distribution, sale, importation, exportation, and possession of cannabis across Canada.
The Minister of Health may appoint inspectors who are empowered to cansdian premises and to seize and detain devices, and may appoint analysts to analyse or examine radiation emitting devices and packaging.
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CANADA: amendments to SOR 98/282 came into force
Sections 90, 92, and of the Act authorize the Minister of Health to: Update Administrative Burden Baseline update It includes a change to any of the following:. Login error when trying to access an account aor. Skip to main content Skip to “About this site” Skip to section menu. It has a spelling mistake. Active Devices Rule medicql It includes a group of such facilities that report to one common management that has responsibility for the activities carried out in those facilities.
The following new regulations will come into force at the same time as the Cannabis Act, on October 17, The Act and regulations ensure the safety of and prevent deception in relation to food, drugs, cosmetics and medical devices by governing their sale and canacian. Please select all that apply: Information is outdated or wrong.
List of Acts and Regulations –
Devixe Rules Rule Near patient in vitro diagnostic device for the detection of pregnancy or for fertility testing. Pesticides include a variety of products regulatons as insecticides, herbicides and fungicides for use in agriculture, forestry, industry and households. Except as authorized by regulation or via an exemption issued under Section 56 of the Act, all activities involving substances listed in the Schedules to the Act, i.
This Act and the Regulations protect human health and the environment through a pre- and post-market evaluation program to prevent unacceptable risks. The Act prohibits a number of activities pertaining to assisted reproduction and related research, including cloning, in vitro embryo sex selection and payment for surrogacy. Report a problem or mistake on this page.
List of Acts and Regulations
Other issue not in this list. Other Uses Rule rebulations Return to footnote a S. Microbiological media used to identify or infer the identity of a microorganism. A medical device that transmits or withdraws energy or a substance to or from a patient without substantially altering the energy or the substance is not an active device. The objectives of the Act are to prevent young persons from accessing cannabis, to protect cevice health and public safety by establishing strict product safety and product quality requirements, and to deter criminal activity by imposing serious criminal penalties for those operating outside the legal framework.
Tissue expanders for breast reconstruction and augmentation. I can’t find what I’m looking for. List of Acts and Regulations.